|OBO ID: DOID:0060786|
|Term Name:||hypomyelinating leukodystrophy||Search Ontology:|
|Definition:||A leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system. (2)|
|Ontology:||Human Disease (DOID:0060786)|
|is a type of:||
OTHER hypomyelinating leukodystrophy PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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